1. Nucleophile and Electrophile Identification a. Which of the following species is likely to behave as a in the box below each species. electrophile? Put your answer nucleophile and which as an CH3O NH4 NO2 Species CN Br Nuc or Elect? CH H-C C-H НО" Species CH3S NH3 Nuc or Elect? b. Draw the following Functional Groups, including lone pairs of electrons. Predict the bond polarity of the functional group using S+ and &- if applicable (think about electronegativity differences!). Then, identify ALL nucleophilic and electrophilic sites using your knowledge of bond polarity. EXAMPLE: Alcohol Aldehyde Amine Acid Chloride Hас-о-н electrophilic electrophilic nucleophilic Alkene Ketone Ether Carboxylic Acid

1. Nucleophile and Electrophile Identification a. Which of the following species is likely to behave as a in the box below each species. electrophile? Put your answer nucleophile and which as an CH3O NH4 NO2 Species CN Br Nuc or Elect? CH H-C C-H НО" Species CH3S NH3 Nuc or Elect? b. Draw the following Functional Groups, including lone pairs of electrons. Predict the bond polarity of the functional group using S+ and &- if applicable (think about electronegativity differences!). Then, identify ALL nucleophilic and electrophilic sites using your knowledge of bond polarity. EXAMPLE: Alcohol Aldehyde Amine Acid Chloride Hас-о-н electrophilic electrophilic nucleophilic Alkene Ketone Ether Carboxylic Acid

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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4. Draw the possible resonance structures for compounds C and D. Include lone pairs and indicate non-zero formal charges. Circle the minor resonance contributor for compound C. O :O: :O: C & D
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Student Name: 2. Find each functional groups in each molecule below. For each functional group indicate the type of compound (Ex. Aldehyde) the functional group represents.orgn normale) sigur GRENSA REVISTA 1olanla isyan yo wao lliw ancite 1ortarw zalb919 HN. NH₂ ora yem elupsion Joide sp HO H wor N SH medans 14 jutuda OH 52 ovibbeldo abnod 10 amate inslofted costs CHO oseOH OH ules and ameldo19 90tang san moldong gniwollat erit sfalqmoj abyd 5310 L
Type here to search JD RK, MZ TB E, SM -) (C) ||| e Man N Classify each of these chemical compounds: WE O PRINCIPLES OF ORGANIC CHEMISTRY Identifying organic compounds vertime for your home. til ste sey Spall On dusty When Calling compound CuCh (CH₂)₂0 CH₂CH₂ Explanation E type of compound (check all that apply) molecular ionic HP Eve Fase RK-burial-sent papers Kelm PS: organic inorganic hydrocarbon molecular X 585-343-8868 9/13 10 am ionic organic inorganic hydrocarbon molecular Check ionic organic inorganic hydrocarbon burial-go ahead HE Turner Batavia Justin Sarith $ AB, TB © 2023 McGraw Hill LLC Christopher Mitche SM- & top appy for arrangement) 17
Name this molecule.
R Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. HH :0: CH3 H H:O Na Select to Add Arrows NaH THF O :0: 4-4 Select to Add Arrows
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A BE M (c) W Chapter... H₂N Type of hydrocarbon: O alkane alkene alkyne arene X Type of structure: straight-chain branch cyclic aromatic X 73,181 4 с tv G ● JUL 26 G
ぐ=m, Part 4: Cycloalkanes and Stereochemistry. assignment. Br Br Br ...|H ...H ... H ..iBr H. Br Br .... ICH3 H. 18. For rings that an the and label each atom as R or S. Some rings will not have an R or S